Variant #0000527703 (NC_000006.11:g.157100043_157100048del, NM_020732.3:c.980_985del (ARID1B))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.157100043_157100048del
DNA change (hg38) g.156778909_156778914del
Published as ARID1B(NM_001374828.1):c.1229_1234del (p.(Gly410_Gly411del))
ISCN -
DB-ID ARID1B_000235
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID1B NM_020732.3 -/. - c.980_985del r.(?) p.(Gly327_Gly328del)


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